DEVICE: VBeam Prima CC Delivery System (00817495023007)
Device Identifier (DI) Information
VBeam Prima CC Delivery System
7123-00-0431
In Commercial Distribution
7123-00-0431
Candela Corporation
7123-00-0431
In Commercial Distribution
7123-00-0431
Candela Corporation
Delivery System Assembly
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
No | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
65509 | Dermatological laser beam producing handpiece |
A hand-held component of a professional, high-powered, dermatological laser system designed to both generate and direct a therapeutic laser (diode laser) for dermatological applications (e.g., hair removal, treatment of dermal lesions). This device is connected to a control unit which supplies power to the handpiece and allows control of the treatment. This is a reusable device.
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Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
GEX | Powered Laser Surgical Instrument |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K230990 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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No Device Sizes |
Device Record Status
6ac9c0e0-8664-4f20-b60b-293153f8a1b9
October 03, 2024
8
December 12, 2019
October 03, 2024
8
December 12, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
800-733-8550
customer.service@candelamedical.com
customer.service@candelamedical.com